Process for cocrosslinking water soluble polymers and products thereof

ABSTRACT

Poly(ethylene oxide) and at least one other water soluble polymer are conveniently cocrosslinked by exposing aqueous systems of the polymers to high energy irradiation. The resulting products are insoluble hydrophilic gels which can contain or when dried absorb large quantities of aqueous fluids and hence are useful as absorbing media for disposable absorbent articles, agricultural applications and the like.

United States Patent Assarsson et al.

PROCESS FOR COCROSSLINKING WATER SOLUBLE POLYMERS AND PRODUCTS THEREOF Inventors: Per Gunnar Assarsson, Montclair,

N.J.; Paul Arliss King. Warwick Assignee'. Union Carbide Corporation, New

York, NY

Filed: Sept. 10, i973 Appl No: 395,553

Related US. Application Data Continuation of Ser. No. 152.370, June ll, I97], abandoned US. Cl. 204/159J2; 128/284; [28/285; 204/l59il4: 260/2 EN; 260/9 R; 260/13; 260/874; 260/895; 260/897 R Int. Cl. H C08d 1/00; C08f l/l6 Field of Search .i 204/l59il4, 159.12; 260/29.6 NR, 874

Aug. s, 1975 [56] References Cited UNITED STATES PATENTS 3,264,202 8/1966 King 204/l59.l4 3,470,078 9/l969 King i. 204/l59rl4 3,664.343 5/[972 Assarsson 204/15914 Primary ExaminerMurray Tillman Assistant Examiner-Richard B. Turer Attorney. Agent, or Firm-W. R Moran [57] ABSTRACT 8 Claims, No Drawings PROCESS FOR COCROSSLINKING WATER SOLUBLE POLYMERS AND PRODUCTS THEREOF This is a continuation of application Ser. No. l52,370 filed June l l, 1971, now abandoned.

This invention relates in general to a process for cocrosslinking water soluble polymers and the products obtained thereby. In one aspect, this invention relates to a process for cocrosslinking poly(ethylene oxide) and at least one other water soluble polymer. In a further aspect, this invention relates to cocrosslinked polymers of poly(ethylene oxide) and other water soluble polymers.

It has been reported in the literature that water solutions of poly(ethylene oxide) can be crosslinked by exposure to ionizing radiation. For example, in U.S. Pat. No. 3,264,202 ethylene oxide polymers were crosslinked by exposure of a solution of the polymer to irradiation to provide a gel-like material which was essentially water insoluble. The gel-like material then can be dried to remove essentially all the water. Due to its ability to absorb large quantities of fluids, crosslink poly- (ethylene oxide) is useful for a wide variety of applications. For instance, it is useful as a plant growth medium as disclosed in U.S. Pat. No. 3,336,129, as a burn and wound dressing as set forth in U.S. Pat. No. 3,419,006 and as a cooling medium as disclosed in U.S. Pat. No. 3,545,230. Prior to the present invention, however, cocrosslinking of poly(ethylene oxide) with other water soluble polymers which do not have the ethylene ether unit has not been reported.

It has now been found that aqueous systems of poly- (ethylene oxide) and other water soluble polymers can be cocrosslinked to provide insoluble hydrophilic gels. in particular, it has been found that heterogeneous systems wherein two or more aqueous phases exists can be cocrosslinked to provide a gel which has a homogeneous appearance and properties which are different from gels prepared by crosslinking solutions of the individual polymers.

It is therefore an object of this invention to provide a process for cocrosslinking water soluble polymers. Another object of this invention is to provide a process for cocrosslinking poly(ethylene oxide) and other water soluble polymers. A further object of this invention is to provide a process for cocrosslinking heterogeneous aqueous systems of water soluble polymers. Another object of this invention is to provide a process for cocrosslinking homogeneous aqueous solutions of poly(ethylene oxide) and water soluble polymers. A still further object is to provide insoluble hydrophilic gels of cocrosslinked water soluble polymers. These and other objects will be readily become apparent to those skilled in the art in the light of the teachings herein set forth.

In its broad aspect, this invention is directed to a process for cocrosslinking water soluble polymers and to the products obtained therefrom. The process of this invention comprises cocrosslinking, such as by irradiation, two or more water soluble polymers selected from the group of non-ionic, cationic and anionic polymers. Illustrative polymers which can be cocrosslinked by the process of this invention include, among others poly- (ethylene oxide) and those from the group (a), consisting of starch, hydroxyethyl cellulose, carboxymethyl cellulose, hydroxymethyl cellulose, hydroxypropyl cellulose, polyvinyl alcohol, polyvinyl pyrrolidone, poly- 2 acrylamide, poly-4-vinyl-n-butylpyridinium bromide, polyvinylmethyl ether, vinylmethyl ether-maleic anhydride copolymer and gelatin or the group (b) consisting of polyacrylic acid, ammonium polyacrylate and ethylene maleic anhydride copolymer. The process comprises the steps of:

a. forming an aqueous soltuion of two or more of the water soluble polymers,

b. adjusting the pH of the solution to within the range of from about 2 to about I l for polymers of group (a), and to within the range of greater than 0.4 and less than 9.0 for the polymers of group (b),

c. intimately mixing the solution to form a homogeneous or heterogeneous micro-phase system, and

d. before any substantial phase separation, exposing the solution to ionizing radiation for a period of time to form a gel-like material.

The cocrosslinked products of this invention, as hereinbefore indicated, are insoluble hydrophilic gels which have a homogeneous appearance and properties which are different from gels prepared by crosslinking solutions of the individual polymers. For instance, it has been observed that films prepared from the gels of this invention, for the most part, have intermediate or greater strength, stability and toughness, compared to films prepared by crosslinking the individual polymers.

In practice, the crocrosslinked, insoluble, hydrophilic gels of this invention are conveniently prepared by forming an aqueous system of poly(ethylene oxide) and at least one of the other water soluble polymers. The majority of the polymers do not form a homogeneous system and hence, the polymer must be cocrosslinked before any substantial phase separation occurs. In order to cocrosslink poly(ethylene oxide) and the polymers of group (a) above, it has been observed that the pH should be within the range of from about 2 to about 1 I. For cocrosslinking of poly(ethylene oxide) and the polymers of group (b) the pH should be greater than 4.0 and less than 9.0.

Mixing of the polymer solution to form a homogeneous or heterogeneous microphase system can be accomplished by a variety of methods. The mixing must be of such a degree to insure that no substantial phase separation occurs before the polymers are cocrosslinked. For example, ordinary laboratory stirrers have been found suitable to achieve the desired results.

Solutions containing various ratios of poly(ethylene oxide) to the other water, soluble polymers have been successfully cocrosslinked. For example, poly(ethylene oxide) can be present in as little as 1 percent, based on the total weight of the combined polymers, or as high as 99 percent.

In practice, the aqueous solutions, prior to cocrosslinking can contain up to about 50 percent by weight of the combined polymers. Preferably, solutions containing from about 1 to about 20 percent are employed.

The water-soluble poly(ethylene oxide) polymers which are cocrosslinked with the other polymers will usually have a molecular weight such that the reduced viscosity of the polymer will be within the range of from about 0.5 to about 75, and higher, and preferably from about 1 to about 60, or an aqueous viscosity of 25C. of from about 225 centipoises measured at a 5 weight percent concentration, to about 12,000 centipoises, and higher measured at a 1 weight percent concentration.

The water-insoluble hydrophilic cocrosslinked polymers are produced by subjecting the above-described water soluble polymers, to sufficient ionizing radiation to crosslink and insolubilize the polymer forming thereby a water-insoluble hydrophilic products. As used herein, the term ionizing radiation" includes that radiation which has sufficient energy to cause electronic excitation and/or ionization in the polymer molecules or in the solvent (where a solvent is employed) but which does not have sufficient energy to affect the nuclei of the constituent atoms. Convenient sources of suitable ionizing radiation are gamma ray-producing radioactive isotopes such as Co and Cs, spent nuclear fuel elements, X-rays such as those produced by conventional X-ray machines, and electrons produced by such means as Van de Graaff accelerators, linear electron accelerators, resonance transformers, and the like. Suitable ionizing radiation for use in the present invention will generally have an energy level in the range from about 0.05 MeV to about 20 MeV.

The irradiation of the non-crosslinked (water soluble) polymers can be carried out in the solid phase or in solution, Solid polymers can be irradiated in the air, in a vacuum, or under various gaseous atmospheres, while irradiation in solution can be carried with the polymers dissolved in water, or in mixtures of water and water-miscible organic solvents, Any conventional method can be used to bring the solid polymer or polymer solution into contact with the ionizing radiation. Suitable methods are well known and understood by those skilled in the art.

The exact amount of ionizing radiation to which the polymers must be subjected depends on a number of variables. In general, when irradiation is carried out at relatively low rates and in the presence of free radical scavengers such as oxygen, extremely high total doses are required to produce the water-insoluble hydrophilic polymers. On the other hand, when the irradiation is carried out under conditions which favor the relatively long existence of the free radicals produced, for example, when the irradiation is carried out with a high dose rate, in the absence of oxygen, or in solution where oxygen is rapidly used up, the formation of water-insoluble hydrophilic polymers take place readily. The preferred method for producing the waterinsoluble hydrophilic polymers is to carry out the irradiation in an aqueous solution of the water-soluble polymers while employing ionizing radiation having an energy level in the range of about 0.10 MeV. to about 20 MeV. at a total dose of between about 0.05 and megarads. In addition to cocrosslinking by ionizing radiation, the polymers can also be cocrosslinked by chemical methods. For example, perioxides such as, acetyl peroxide, in the presence of a multifunctional reagent such as, divinylbenzene, have been successfully employed.

The terms insoluble or insolubilize as employed throughout the specification are utilized herein to refer to the formation of a product, a variable portion of which is essentially insoluble in water, depending upon the degree of crosslinking. By the term "cocrosslinking" is meant insolubilization of the polymeric mixture wherein like or dislike polymer chains are linked by covalent bonding at one or more cities along the chain. Certain of the polymers may become entrapped in and among the crosslinked polymers without actually being linked themselves. This entrapment will also contribute to the insolubility of the polymers. These polymers can swell and adsorb many times their weight in water because they are also hydrophilic.

The insoluble, hydrophilic cocrosslinked polymers or gels which are prepared by the process of this invention are useful in a wide variety of fields. For example, the gels can contain, or when dried absorb, large quantities of aqueous fluids and hence are useful as absorbing media for disposable absorbent articles, agricultural applications, such as moisture retainers, and the like. They are of particular interest as an absorbing media for diapers, or catamenial devices such as sanitary napkins and tampons.

Although disposable absorbent articles for the absorption of body fluids have been in use for many years they have not always been completely satisfactory to the user. Numerous materials, variations in construction, and absorbents have all been reported in the literature. However, many products currently on the market suffer from the disadvantage of having poor or inferior absorption properties. In the past, the usual method employed to increase absorption characteristics was to add inexpensive materials which had modest or low absorptive capacity such as fluffed wood pulp and the like contained between layers of moisture permeable fabrics. While satisfactory as absorbents for fluids, in many instances, the article would be bulky and not comfortable. For example, diapers must have a minimum thickness to insure sufficient absorption of body fluids. If, however, the absorbing material has a low absorptive characteristic to be acceptable, the diaper would undoubtedly be bulky and not conform properly to the body contours.

Moreover, one of the major disadvantages of the products commercially available today, is that while they may have relatively high absorptive capacities, the absorbing media, if subjected to pressure, can release a portion of the absorbed liquid. This is due to the fact that the liquid is physically entrapped within a fibrous structure and a relatively slight pressure is all that is needed to cause the absorbent media and the liquid to separate. This, of course, is highly undesirable, particularly in catamenial devices.

The insoluble hydrophilic polymers prepared by the process of this present invention, are particularly useful because they possess the ability to incorporate very large amounts of water in the order of 25 to 1000 times their dry weight. Moreover, in addition to possessing the ability to incorporate large amounts of water, they are insoluble in water irrespective of temperature and will retain liquids, solutions and suspensions. ln general, the aforementioned gels are useful for increasing the absorbency of any known or commercially available disposable, article. For example, the hydrogels can be incorporated into diapers of the type disclosed in U.S. Pat. Nos. 2,788,003; 2,860,637; 3,306,293; and 2,667,l68, Similarly, they can be incorporated into tampons or sanitary napkins of the type disclosed in U.S. Pat. Nos. 3,121 3,121,427; 3,070,095 and the like. The gels can be employed in a wide variety of ways, such as, for example, as a powder dispersed in and bonded to a cellulosic similar substrate, or as a film of the hydrogel sandwiched between layers of the supporting structure. Any of the several known methods can be employed to affix the film or powdered hydrogel to the substrate.

In general. the amount of hydrophilic polymer em ployed will be dependent upon the particular absorbent article and its intended use. In practice, it has been observed that disposable absorbent articles can be pre- 6 QP lOO-M from Union Carbide Corporation), Different weight ratios (poly(ethylene oxide) 1 hydroxyethyl cellulose) of 9:l, 3:l, l:l and 1:9 were prepared by simple addition of appropriate volumes under stirring pared containing from about 2 to about 98 weight per- 5 until a homogeneous blend was obtained. cent. of said hydrophilic polymers, based on the total At least five portions of IO cubic centimeters of each weight of said article. weight ratio mixture were poured into standard plastic In some instances, it may be desirable to stabilize the petri dishes and each dish irradiated using a van de cocrosslinked products prepared by the process of this Graff electron accelerator having an energy of 1 MeV invention. It has been observed that poly(ethylene im- 10 to different total doses of 0.2, 0.4, 0.6, 0.8 and 1.0 ine) is an excellent stabilizer. These are polymers pre- Mradh radiat d mixture was allowed to dry in pared from ethylene imine and whi h t i i a ambient room temperature and humidity conditions major amount the recurring unit; overnight. The resulting dry films were each analyzed for per cent insolubilized and saline water absorption capacity in the following manner: {NHCH CH a. percent insoluble: about 0.2 grams of the dried I I polymer is accurately weighed out and placed in jars and in a minor am l l th recurring llmti containing 200 cubic centimeters of a 10 percent water in methanol mixture. The jar is then placed on a roller CHWCH mill for constant agitation for approximately 16 to 20 hours after which time the swollen gel is placed in a CH -CH-J' drying oven. The dried solid is weighed and the per cent insolubilized gel calculated in accordance with the In practice poly(ethylene imine) polymers having mof ll i equation; lecular weights of from about l0,000 to about l00,000 are ideally suited for use in the instant invention. Particularly preferred are the poly(ethylene imine) polynomemacmble weigh mers having molecular weight of from about 20.000 to originm Wight 109 Percent insoluble g about 80,000. These polymers are prepared by pro- $65568 known in literature and are Commercial)! conversely, the extracted material or percent soluble available. content is calculated as follows:

In practice, the poly(ethylene imine) stabilizer is employed in a stabilizing amount. By the term stabilizing amount" as employed throughout the specification and I claims. is meant that quantity of poly( ethylene imine) W 100 percent soluble Comem which when admixed with the polymer will decrease ongm the rate of dfa'gradanon Over that 0f unsmblhzed In cases where the cocrosslinked dried polymer was polymer. It has been observed that as little as about not soluble in this methanobwat r ext t 0.0l weight percent based on the solid polymer, will efure water was em '0 d t {2 mix ure fectively stabilize the polymer against degradation. of 40 s p ye ms ea e same Pmce' from about 0.2 to about 3.0 weight percent is pre- 2 f h ferred. However. if desired, concentrations of poly- S grams 0 t r' accurate (ethylene imine) as high as 50 weight percent can be ed out and Placed m a Jar contammg 200 Cubic employed. centimeters of saline water (0.3 NaCl) and placed on a roller mill for constant agitation for about 16 to 20 EXAMPLE I hours after which time the swollen gel is weighed blot- A Stock Solution of poly(ethylene Oxide) was ting excess water from the gel with tissue. The absorppared by using a commercial coagulant grade resin sold capacity Calculated as follows: by Union Carbide Corporation under the trademark POLYOX" and having a molecular weight in excess of 10. This resin was dissolved by stirring in water to Weight of Swollen Gel give a concentration of 4 percent then shearing the rer ginal Sample Weight absmpm" capuc'ty sulting high viscosity solution in a high speed mixing device to a viscosity of 560,000 cps. In a similar manner, the absorption capacities of a A stock solution of hydroxy ethyl cellulose was also number of other systems were obtained and the values prepared by using a commercial grade resin (Cellosize presented in Table l and ll below:

TABLE I PROPERTIES OF COCROSSLlNKED POLY(ETHYLENE OXlDE) AND OTHER WATER SOLUBLE POLYMERS RATIO BY WEIGHT OF POLYtEl'HYLENE OXIDE) TO OTHER POLYERS Dosein 9:l 3:] lzl 1:3 1:9

Water Soluble Polymer Megarads '4 Gel C up 7% Gel Cap 7c Gel Cap 70 Gel Cap 92 Gel Cap Experimental Starch .8 85 30 83 27 72 23 47 21 25 5 ,6 79 38 82 27 73 29 48 22 l2 l4 .4 78 43 77 39 58 27 49 23 l3 l2 .2 55 72 S6 51 46 39 28 l5 l4 Starch .8 8(1 32 86 27 78 23 67 37 33 l28 TABLE l-Continued PROPERTIES OF COCROSSLINKED POLY(ETHYLENE OXIDE) AND OTHER WATER SOLUBLE POLYMERS RATIO BY WEIGHT OF POLY(ETHYLENE OXIDE) TO OTHER POLYERS Dose in 9:l 3:l l:l l:3 I19 Water Soluble Polymer Megurads 7r Gel Cap 7: Gel Cap 71 Gel Cap 1: Gel Cap 7% Gel Cap Hydrnxyethylcellulose .8 89 29 83 20 83 22 82 19 (OP 30,000) .6 86 39 80 24 77 24 .2 66 I 64 66 55 78 48 69 Hydroxyethylcellulose .8 90 29 88 27 S9 21 83 21 86 I6 (OP I00M) .6 84 42 85 36 86 28 80 23 .2 68 92 4I 28 67 67 66 69 62 57 Carboxymethylcellulose .8 86 32 82 32 80 32 66 29 .2 59 85 56 77 46 88 41 89 I8 93 Ethylene-maleic Anhydride 1.0 95 22 90 19 89 l l 99 25 SI 37 copolymer .8 90 25 88 2O 84 1 l 95 37 6| 50 Ammonium Polyacrylate .8 85 24 86 22 90 22 88 29 77 46 .2 48 50 55 62 5] 64 76 44 84 Polyacrylamide .8 86 28 TABLE II PROPERTIES OF COCROSSLINKED POLY(ETHYLENE OXIDE) AND OTHER WATER SOLUBLE POLYMERS RATIO BY WEIGHT OF POLY(ETHYLENE OXIDE) TO OTHER POLYMERS Dose in 9:1 6:l 4:1 2:]

Water Soluble Polymer Megarads Gel Cap 75 Gel Cap 7: Gel Cap Gel Cap Ethylene-maleic anhydride .2 22 90 63 80 copolymer (5 per cent .4 60 66 58 71 42 64 63 9I aqueous solution pH 4.5) .6 69 46 72 51 65 69 .8 8O 27 75 4O 77 42 76 49 Ethylene-maleic anhydride .2 45 I22 I6 264 copolymer (10 per cent .4 4I 76 53 70 5] 80 58 I36 aqueous solution -pH 4.5) .6 67 54 68 48 71 64 66 82 .8 7l 42 80 41 77 50 74 6| Polyvinyl methylether (l0 .2 per cent aqueous solution) .4 48 67 28 70 47 81 59 The following Examples are illustrative:

EXAMPLE II A 4 percent stock solution of poly(ethylene oxide) was prepared by dissolving an appropriate amount of coagulant grade poly( ethylene oxide), sold under the trademark POLYOX" by Union Carbide Corporation; in water under agitation and then shearing the resulting solution to a viscosity of about 500,000 cps.

A 2 percent stock solution of poly-4-vinyl-n-butyl pyridinium bromide was prepared by dissolving an appropriate amount of the polymer in water under agita tion. The polymer was obtained from the reaction of poly-4-vinyl pyridine with excess n-butyl bromide in ethanol according to known literature synthesis. Twenty grams of 4 percent poly(ethylene oxide) solution was mixed with l 1 grams of 2 percent poly-4-vinyln-butyl pyridinium bromide solution. To obtain a mixture that had a monomer mole ratio of I5: I (polyethylene oxide: poly-4-vinyl-n-butyl pyridinium bromide). Three grams of this mixture having a pH of 4.9 were poured into a plastic petri dish and irradiated with a 1 MeV van de Gralf electron accelerator to a total dose of 0.7 Mrad. The resulting gel was transferred to a beaker from the dish and allowed to equillibrate with excess water for 24 hours. After this time the gel was weighed and its absorption capacity calculated in accordance with the equation:

weight swollen gel calculated solid content in 3 grams solution absorption capaclly In another case the pH of the solution mixture was adjusted by addition of (a) 0.1 N HCl to pH 3 and (b) 0.1 N NaOH to pH 7. Three grams of each of the pH adjusted solution mixtures were irradiated with a 1 MeV van de Graff electron accelerator to a total dose of 0.7 Mrad. The resulting gels were placed in a beaker with excess water and allowed to equillibrate for 24 hours after which time the gels were weighed and the absorption capacity calculated as above. In a similar manner, the absorption capacities of a number of other systems were obtained and the values presented in Table III below. The water soluble polymers which were cocrosslinked with poly(ethylene oxide) are set forth in the first column.

TABLE I11 GEL CAPACITY E H O MONOMER gm solid COMPOSITION MEGA- MOLE pH 1N WATER AFTER 24 HOURS RADS RATIO PEO-Polyethylene- .7 15:1 8.4 9]

imine (l) 3.7 89 .7 l 8.2 67 4.6 87 PEO-Poly-4-vinyl-n- .7 15:1 3.0 130 butylpyridinium bromide 49 960 7.0 630 .7 20:1 3.0 130 7.0 890 .7 40:1 3.0 100 6.3 235 7.0 410 1.0 20.1 5.5 469 10.0 416 1.0 4011 6.1 166 10.4 158 PEO-Polyvinyl- 1.0 20:20z1 5.5 365 alcohol poly- 4-vinyl-n-butyl pyridinium bromide PEO-Polyvinyl- 1.0 20:20:1 7.4 60

alcoholpolyethyleneimine PEO'PolyvinyL 2.0 20:1 7 4 44 alcohol-polyethyleneimine 3.3 57 2.0 40z| 7.1 46 3.0 53 PEO-Polyviny- 2.0 20:1 5.4 592 alcohol-poly- 4-vinyl-n-butyl- 10.6 324 pyridinium bromide 2.0 40:1 5.4 330 PEO represents (1 l Poly(ethylene oxide) 9.9 258 EXAMPLE Ill A stock solution of poly(ethylene oxide) was pre pared by using a commercial grade resin sold by Unior Carbide Corporation under the trademark POLYOX coagulant resin and having a molecular weight in excess of 10". This resin was dissolved by stirring in water to give a concentration of about 10 percent then shearing the resultant high viscosity solution in a high speed mixing device to a viscosity of about 1,000,000 cps.

A stock solution of ammonium polyacrylate (commercial grade WS 851 from B. F. Goodrich Chem. Company) was prepared by dissolving this resin in water while stirring to a concentration of about 10 percent. Mixtures of both resin solutions were prepared at weight ratios (poly(ethylene oxide) ammonium polyacrylate) of 4:1 and 8:1 were prepared by addition 01 appropriate volumes of each solution while stirring until a homogeneous blend was obtained.

Each weight ratio mixture was spread out on a polyethylene film backing and the thickness of the solution mixture adjusted with a doctor blade to a wet thickness of approximately 10-12 mils which gave a dry film of about 1 mil thickness. The solution mixture was passed under a van de Graff electron accelerator having an energy of 1.5 MeV and irradiated total doses of 0.4. 0.5 and 0.6 Mrad. Each irradiated mixture was allowed to dry at ambient room temperature and humidity conditions overnight. The resultant films were each analyzed for per cent insolubilized gel content and saline water absorption capacity as outlined in Example 11.

In a similar manner irradiated films were prepared of poly(ethylene oxide) mixtures with poly(acrylic acid) adjusted to pH 4.5 and poly-4-vinyl-n-butyl pyridinium 40 bromide. The results are tabulated in Table IV below:

TABLE IV PROPERTIES OF CO-CROSSLINKED Although the invention has been illustrated by the preceding examples, it is not to be construed as being limited to the materials employed therein. but rather. the invention encompasses the generic area as hereinbefore disclosed. Various modifications and embodimerits of this invention can be made without departing from the spirit and scope thereof.

What is claimed is:

l. A process for cocrosslinking at least two water soluble polymers one of which is poly(ethylene oxide) and the other is starch, said process comprising the steps of:

a. forming an aqueous solution comprising up to 50 percent by weight of poly(ethylcnc oxide) and starch,

b. adjusting the pH of said solution to within the range of from about 2 to about 1 1.

c. intimately mixing said solution to form a homogencous or heterogeneous micro-phase system. and

d. before any substantial phase separation, exposing said solution to ionizing radiation of a sufficient dosage and for a period of time to form a gel.

2. The cocrosslinked product of claim 1. 

1. A PROCESS FOR COCROSSLINKING AT LEAST TWO WATER SOLUBLE POLYMERS ONE OF WHICH IS POLY(ETHYLENE OXIDE) AND THE OTHER IS STARCH SAID PROCESS COMPRISING THE STEPS OF: A. FORMING AN AQUEOUS SOLUTION COMPRISING UP TO 50 PERCENT BY WEIGHT OF POLY(ETHYLENE OXIDE AND ATARCH B. ADJUSTING THE PH OF SAID SOLUTION TO WITHIN THE RANGE OF FROM ABOUT 2 TO ABOUT 11, C. INTIMATELY MIXING SAID SOLUTION TO FORM A HOMOGENEOUS OR HETEROGENEOUS MICRO-PHASE SYSTEM AND D. BEFORE ANY SUBSTANTIALLY PHASE SEPARATION EXPOSING SAID SOLUTION TO IONIZING RADIATION OF A SUFFICIENT DOSAGE AND FOR A PERIOD OF TIME TO FORM A GEL
 2. The cocrosslinked product of claim
 1. 3. An absorbent product prepared by drying the cocrosslinked product of claim 1 to remove at least some of the water.
 4. A disposable absorbent article containing at least one of said gels prepared by the process of claim
 1. 5. The disposable absorbent article of claim 4 which is a catamenial device.
 6. The disposable absorbent article of claim 4 which is a sanitary napkin.
 7. The disposable absorbent article of claim 4 which is a tampon.
 8. The disposable absorbent article of claim 4 which is a diaper. 